ZA201800765B - Process for preparing parp inhibitor, crystalline forms, and uses thereof - Google Patents

Process for preparing parp inhibitor, crystalline forms, and uses thereof

Info

Publication number
ZA201800765B
ZA201800765B ZA201800765A ZA201800765A ZA201800765B ZA 201800765 B ZA201800765 B ZA 201800765B ZA 201800765 A ZA201800765 A ZA 201800765A ZA 201800765 A ZA201800765 A ZA 201800765A ZA 201800765 B ZA201800765 B ZA 201800765B
Authority
ZA
South Africa
Prior art keywords
crystalline forms
parp inhibitor
preparing
preparing parp
inhibitor
Prior art date
Application number
ZA201800765A
Inventor
Hexiang Wang
Bo Ren
Xianzhao Kuang
Changyou Zhou
Original Assignee
Beigene Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beigene Ltd filed Critical Beigene Ltd
Publication of ZA201800765B publication Critical patent/ZA201800765B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/22Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)
ZA201800765A 2015-08-25 2018-02-06 Process for preparing parp inhibitor, crystalline forms, and uses thereof ZA201800765B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2015088003 2015-08-25
PCT/CN2016/096200 WO2017032289A1 (en) 2015-08-25 2016-08-22 Process for preparing parp inhibitor, crystalline forms, and uses thereof

Publications (1)

Publication Number Publication Date
ZA201800765B true ZA201800765B (en) 2019-10-30

Family

ID=58099633

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA201800765A ZA201800765B (en) 2015-08-25 2018-02-06 Process for preparing parp inhibitor, crystalline forms, and uses thereof

Country Status (15)

Country Link
US (1) US10457680B2 (en)
EP (1) EP3341375B1 (en)
JP (1) JP6940039B2 (en)
KR (1) KR20180041748A (en)
CN (2) CN112521390A (en)
AU (1) AU2016312011B2 (en)
BR (1) BR112018003634B1 (en)
CA (1) CA2994895A1 (en)
EA (1) EA037366B1 (en)
IL (2) IL296835A (en)
MX (1) MX2018002322A (en)
NZ (1) NZ739876A (en)
TW (1) TWI736550B (en)
WO (1) WO2017032289A1 (en)
ZA (1) ZA201800765B (en)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK2797921T3 (en) 2011-12-31 2017-10-02 Beigene Ltd FUSED TETRA- OR PENTA-CYCLIC DIHYDRODIAZEPINOCARBAZOLONES AS PARB INHIBITORS
US10457680B2 (en) 2015-08-25 2019-10-29 Beigene, Ltd. Process for preparing a PARP inhibitor, crystalline forms, and uses thereof
EP3519051B1 (en) * 2016-09-27 2021-09-22 Beigene, Ltd. Treatment of cancers using combination comprising parp inhibitors
US10899763B2 (en) 2017-02-28 2021-01-26 Beigene, Ltd. Crystalline forms of salts of fused penta-cyclic dihydrodiazepinocarbazolones, and uses thereof
WO2018165615A1 (en) * 2017-03-09 2018-09-13 The Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Parp-1 and methods of use thereof
WO2019015561A1 (en) * 2017-07-17 2019-01-24 Beigene, Ltd. Treatment cancers using a combination comprising parp inhibitors, temozolomide and/or radiation therapy
MX2020012259A (en) 2018-05-18 2021-01-29 Novartis Ag Crystalline forms of a tlr7/tlr8 inhibitor.
US20210205323A1 (en) * 2018-06-01 2021-07-08 Beigene, Ltd. Maintenance therapy of a parp inhibitor in treating gastric cancer
USD926356S1 (en) * 2019-03-14 2021-07-27 Tuanfang Liu Battery for electronic cigarette
CN113004279B (en) * 2019-05-10 2023-01-06 百济神州(苏州)生物科技有限公司 Method for controlling water content of PARP inhibitor-containing sesquihydrate product
CN111171001B (en) * 2019-05-16 2022-04-29 百济神州(苏州)生物科技有限公司 Crystallization method of PARP inhibitor intermediate
CN111171002B (en) * 2019-05-16 2021-04-06 百济神州(苏州)生物科技有限公司 Preparation method of PARP inhibitor intermediate
MX2021014339A (en) 2019-05-31 2022-01-06 Beigene Ltd Parp inhibitor pellet preparation and preparation process therefor.
CN112007011B (en) * 2019-05-31 2024-07-23 百济神州(苏州)生物科技有限公司 PARP inhibitor pellet capsule and preparation process thereof
WO2021046014A1 (en) 2019-09-03 2021-03-11 Teva Czech Industries S.R.O Solid state forms of pamiparib and process for preparation thereof

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1140936E (en) 1999-01-11 2004-06-30 Agouron Pharma TRICYLIC POLYMER INHIBITORS (ADP-RIBOSE) POLYMERASES
AU3652102A (en) * 2000-12-01 2002-06-11 Guilford Pharm Inc Compounds and their uses
EA009337B1 (en) * 2003-01-09 2007-12-28 Пфайзер Инк. Tricyclic compounds as kinase inhibitors for increasing effectiveness of an anti-neoplastic agent or therepeutic radiation
CN102171214B (en) 2008-08-06 2015-06-24 生物马林药物股份有限公司 Dihydropyridophthalazinone inhibitors of poly(ADP-ribose)polymerase (PARP)
DK2797921T3 (en) * 2011-12-31 2017-10-02 Beigene Ltd FUSED TETRA- OR PENTA-CYCLIC DIHYDRODIAZEPINOCARBAZOLONES AS PARB INHIBITORS
CN112457403B (en) 2013-09-13 2022-11-29 广州百济神州生物制药有限公司 anti-PD 1 antibodies and their use as therapeutic and diagnostic agents
KR102130600B1 (en) 2014-07-03 2020-07-08 베이진 엘티디 Anti-PD-L1 Antibodies and Their Use as Therapeutics and Diagnostics
US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
US10457680B2 (en) 2015-08-25 2019-10-29 Beigene, Ltd. Process for preparing a PARP inhibitor, crystalline forms, and uses thereof
EP3519051B1 (en) * 2016-09-27 2021-09-22 Beigene, Ltd. Treatment of cancers using combination comprising parp inhibitors
US10899763B2 (en) 2017-02-28 2021-01-26 Beigene, Ltd. Crystalline forms of salts of fused penta-cyclic dihydrodiazepinocarbazolones, and uses thereof
WO2019015561A1 (en) 2017-07-17 2019-01-24 Beigene, Ltd. Treatment cancers using a combination comprising parp inhibitors, temozolomide and/or radiation therapy
CN113004279B (en) * 2019-05-10 2023-01-06 百济神州(苏州)生物科技有限公司 Method for controlling water content of PARP inhibitor-containing sesquihydrate product

Also Published As

Publication number Publication date
EA037366B1 (en) 2021-03-18
IL296835A (en) 2022-11-01
BR112018003634A2 (en) 2018-11-21
CN112521390A (en) 2021-03-19
AU2016312011A1 (en) 2018-03-08
IL257442B2 (en) 2023-03-01
KR20180041748A (en) 2018-04-24
US20190177325A1 (en) 2019-06-13
EP3341375B1 (en) 2022-04-13
MX2018002322A (en) 2018-04-11
IL257442A (en) 2018-04-30
US10457680B2 (en) 2019-10-29
IL257442B (en) 2022-11-01
CA2994895A1 (en) 2017-03-02
BR112018003634B1 (en) 2023-11-21
WO2017032289A1 (en) 2017-03-02
EA201890547A1 (en) 2018-07-31
EP3341375A4 (en) 2019-01-16
BR112018003634A8 (en) 2023-01-17
JP2018528199A (en) 2018-09-27
EP3341375A1 (en) 2018-07-04
TW201718586A (en) 2017-06-01
JP6940039B2 (en) 2021-09-22
CN107922425A (en) 2018-04-17
CN107922425B (en) 2021-06-01
NZ739876A (en) 2022-09-30
TWI736550B (en) 2021-08-21
AU2016312011B2 (en) 2021-02-04

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